EP1146025B1 - Wc-base composite ceramic sintered compact - Google Patents
Wc-base composite ceramic sintered compact Download PDFInfo
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- EP1146025B1 EP1146025B1 EP00970077A EP00970077A EP1146025B1 EP 1146025 B1 EP1146025 B1 EP 1146025B1 EP 00970077 A EP00970077 A EP 00970077A EP 00970077 A EP00970077 A EP 00970077A EP 1146025 B1 EP1146025 B1 EP 1146025B1
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- sintered body
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/64—Burning or sintering processes
- C04B35/645—Pressure sintering
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/515—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
- C04B35/56—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides
- C04B35/5603—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides with a well-defined oxygen content, e.g. oxycarbides
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/515—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
- C04B35/56—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides
- C04B35/5607—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on refractory metal carbides
- C04B35/5626—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on refractory metal carbides based on tungsten carbides
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/64—Burning or sintering processes
- C04B35/645—Pressure sintering
- C04B35/6455—Hot isostatic pressing
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T407/00—Cutters, for shaping
- Y10T407/27—Cutters, for shaping comprising tool of specific chemical composition
Definitions
- the present invention relates to a WC-based composite ceramics sintered body used in sliding wear parts of a machine, edged tools for cutting polymer materials such as polyethylene or metals such as aluminum alloys, press dies for bending and cutting metals or polymer materials, or the like which are required to have a high wear resistance.
- Japanese Patent Publication No. Hei 01-024747 Japanese Patent Laid-Open Publication No. Sho 58-120571
- Japanese Patent Laid-Open Publication No. Hei. 03-051667 Japanese Patent Laid-Open Publication No. Hei 09-221352 disclose die materials in which ZrO 2 ceramics is strengthened by dispersing carbide or nitride grains of transition metals therein.
- Required properties of the die material in case of applying ceramics to sliding wear parts, cutting blades or dies include four parameters of Young's modulus, hardness, heat conductivity and electrical workability.
- each conventional material is insufficient in stiffness during its high-speed sliding motion with respect to an opposite member. This causes an elastic deformation of the material and excessive friction between the material and the opposite member, resulting in an abnormal wear of the material.
- the ferrous materials cause an abnormal wear, while in ZrO 2 -based materials, the resulting frictional heat promotes crystal transformation and thereby an undesirable wear arises from fall-off of grains. This wear has an influence on usable period or life of parts. In particular, such wear would be a fatal factor in a field having a requirement of accurate motion.
- the advantage of ceramics compared to conventional metal-based materials is to provide an improved wear resistance based on high hardness.
- a ceramics-based die material including zirconia as a primary component is insufficient in hardness and thereby low wear resistance or short life is undesirable exhibited.
- WC includes free carbon.
- the free carbon remains in a sintered body, and undesirable fracture can originate in the remaining free carbon, resulting in lowered strength of the sintered body.
- ZrO 2 and WC have different thermal expansion coefficients and are oxide and carbide, respectively, which are not solid-soluble each other.
- heat conductivity when heat conductivity is low, heat generated by friction during high-speed motion can be accumulated in the material, and this accumulated heat causes phase transition in zirconia as the primary component, resulting in fracture due to the transformation.
- US 5,994,250 discloses a sintered ceramic body which can be worked by electrical discharge machining which can be worked into sintered ceramic tools.
- the present invention provides a WC-based composite ceramics sintered body according to claim 1. Preferred embodiments are disclosed in the subclaims. According to the invention is also a method according to claim 5.
- the WC-based composite ceramics sintered body can be obtained by the following process.
- a pre-sintered prepared powder of raw material is held in an atmosphere containing oxygen in a temperature range of 200°C to 600°C for 0.1 hour to 3 hours to provide WC grains including solid-solved oxygen represented by a chemical formula of WC x O y (where 0.005 ⁇ y / x + y ⁇ 0.05).
- partially stabilized ZrO 2 is used which includes one or more of stabilizers selected from the group consisting of Y 2 O 3 , CeO 2 and MgO.
- the obtained WC is subjected to a normal sintering process or hot press sintering process in an inert gas in a temperature range of 2023 K to 2123 K to obtain the WC-based composite ceramics sintered body.
- a normal sintering process or hot press sintering process in an inert gas in a temperature range of 2023 K to 2123 K to obtain the WC-based composite ceramics sintered body.
- free carbon in the WC grains is removed to provide an improved grain fall-off resistance, and an enhanced hardness, toughness and strength of the composite material.
- the electrical machining operation can provide an improved electrical workability and heat conductivity with lower electric resistance.
- a compound of raw material shown in Table 1 was prepared by providing a WC powder having an average grain size of 0.5 ⁇ m, and a predetermined amount of ZrO 2 having an average grain size of 0.5 ⁇ m and partially stabilized by 3 mol % of Y 2 O 3 , as primary components, adding the predetermined amount of ZrO 2 to the WC powder, and mixing the WC powder and the predetermined amount of ZrO 2 for 20 hours within a nylon pot containing ZrO 2 balls each comprising a sintered body having a purity of 99.5 % in a methanol solvent. The resulting slurry was taken out, and a granular powder was then prepared by adding an alcoholic binder to the slurry, and drying the slurry with the binder by a closed cycle type spray dryer in a nitrogen atmosphere.
- Samples for a bending test of 4 x 5 x 45 and samples for measuring heat conductivity of ⁇ 20 x 3 t mm were made from the prepared granular powder through die press working, and were degreased by holding in a vacuum atmosphere at 500°C for 1 hour. After degreasing, the resulting press bodies were subjected to a heat treatment in an ambient atmosphere at 400°C for 1 hour to introduce oxygen into the WC grains. Then, the bodies were subjected to a normal sintering process in an argon gas in a temperature range of 2030 K to 2123 K. A part of the obtained samples were subjected to an HIP treatment using a nitrogen gas in a temperature range of 1923 K to 2023 K. Otherwise, the oxidizing heat treatment may be carried out to the powder of raw material or the prepared powder after granulating and drying to obtain the same effect.
- the degreased press bodies of 50 x 50 x 5 mm were put in a carbon dice and subjected to the hot press sintering process. Each sample made through two kinds of sintering processes was machined, and each heat conductivity of their mechanical properties was measured.
- the obtained samples were appropriately cut to research their solid-state properties and measure their thermal properties such as heat conductivity.
- the ratio of C and O was determined by measuring each diffractive intensity of WC and WO 3 at a low angle side in X-ray diffractions of the obtained sintered bodies.
- WC grains have excellent properties of high hardness, Young's modulus, conductivity and melting point. On the other hand, due to its poor sintering property, a single substance of WC is hardly to be adequately sintered.
- a binder phase is formed by adding a metal such as Co or Ni to finalize a sintered body structure.
- the properties of metals serving as the binder phase are significantly exhibited in evaluations of wear resistance, high temperature property which are influenced by hardness or the like.
- using ZrO 2 which has high strength and toughness among ceramics, as a substitute for the binder phase based on metals, such as Co or Ni, allows the WC grains to be sintered in approximate theoretical density.
- the content of WC depends on the sintering property varied by the addition amount of ZrO 2 , and it has been identified that a dense sintered body exhibiting high strength could be obtained by adding ZrO 2 of 20 volume %.
- the ZrO 2 component is preferably provided as a stabilized ZrO 2 obtained by adding Y 2 O 3 of 2 to 4 mol %
- a stabilized ZrO 2 obtained by adding MgO or CeO 2 may achieve the similar effects.
- a sufficient sintering property cannot be assured by 20 volume % or less of ZrO 2 .
- a sintered body having many pores will be provided with degraded strength and hardness.
- 60 volume % or more of ZrO 2 it has been identified that the properties of ZrO 2 was significantly exhibited, and caused deteriorated hardness and wear resistance, and the grain fall-off, particular to ZrO 2 , due to transformation by the frictional heat, resulting in inferior sliding wear resistance.
- WC includes free carbon.
- the free carbon is apt to remain in the form of a lump of carbon in a sintered body, and some fracture can originate in the remaining free carbon, resulting in lowered strength of the sintered body.
- the free carbon is removed by subjecting WC in the stage of green compact to an oxidizing heat treatment to sublimate the free carbon as a hydrocarbon compound, which enables a sintered body to assure high strength.
- the inventive examples No. 1 to 9 show a minimum strength decreasing rate of 15 % or less. While the examples No. 16 to 19 having the same composition as that of the inventive examples but the heat treatment conditions out of the inventive range show few difference in most properties, their minimum strength is lower and a decreasing rate of 25 % or more is caused by a remaining free carbon.
- WC is gradually oxidized in the temperature range of less than 600°C and the oxidization exponentially accelerates in the temperature range of 600°C or more.
- the solid solution amount of oxygen is increased.
- the value of y / x + y in WC x O y is increased to 0.05 or more, an oxide film is formed on the surface of the WC. This causes lowered strength. Further, since the oxide film has an insulative property, the electrical conductivity is deteriorated.
- the solid-solution amount of oxygen to WC is defined by WC x O y (where 0.005 ⁇ y / x + y ⁇ 0.05).
- thermal expansion coefficients of WC and ZrO 2 are 4 x 10 -6 and 10 x 10 -6 , respectively.
- thermal expansion coefficients of WC and ZrO 2 are 4 x 10 -6 and 10 x 10 -6 , respectively.
- ceramics is densified in solid-phase sintering, not in liquid-phase sintering, during a sintering process.
- solid-phase sintering between Al 2 O 3 and WC Al 2 O 3 acts as a rate-limiting factor of sintering.
- any plastic flow is caused during crystal structure is densified, and thereby pores are apt to remain.
- WC x O y and ZrO 2 according to the present invention, a superplasticity phenomenon appears in the sintering temperature of ZrO 2 , and a structure in which ZrO 2 gets into a space between crystals is formed to provide enhanced density.
- the density is more enhanced by using WC x O y which includes a few amount of solid-solved oxygen, as compared with using only WC.
- an adequate sintering can be achieved by less amount of ZrO 2 than that in combination of only WC and ZrO 2 .
- WC x O y and ZrO 2 grains are dispersed in an individually independent form without any mutual reaction. Further, since WC x O y is matrix and ZrO 2 functions to restrain grain growth as with the function of a grain boundary binding phase. This allows WC and ZrO 2 to be uniformly dispersed respectively. In addition, by virtue of generation of residual stress, as compared to conventional ceramics, enhanced values of strength, toughness and hardness are exhibited. More excellent thermal and electrical properties than ever are also provided.
- the composite material has a Young's modulus of 300 MPa or more, which is 1.5 times or more of that of ZrO 2 -based ceramics or metals, and can assure the same stiffness as that of Si 3 N 4 .
- this composite material is applied to high-speed motion mechanisms such as bearing and sleeve, or high-speed press machines, lowered distortion and deformation, restrained frictional heat, and reduced sliding wear can be achieved.
- ceramics including a large amount of ZrO 2 has low heat conductivity.
- the composite material according to the present invention includes WC having high heat conductivity as a primary component, a sufficient heat conductivity being ten times of that of a simple substance of ZrO 2 is obtained to provide an improved thermal shock resistance against rapid heating and cooling.
- WC x O y itself has a high conductivity. Thus, larger WC x O y amount, less electric resistance value.
- an electrical machining such as a wire-cut electric discharge machining can be applied to a composite material including 30 volume % or more of WC x O y . In this case, it has been proved that surface roughness of the electrically machined surface was influenced by the conductivity of the composite material and the dispersed degree of conductive grains. As shown in Table 1, it has been identified that 50 volume % or more of WC x O y could provide an improved surface roughness of the electrically machined surface.
- each agglomerate of WC x O y and ZrO 2 is required to limit to 10 ⁇ m or less when converting into diameter of the same area, and to 3 or less per mm 2 in its number.
- each wear value was measured by inserting each sample of the inventive materials and comparative materials each having an outer diameter of 40 mm, inner diameter of 30 mm and a length of 50 mm, into an inside of a hard metal cylinder having an outer diameter of 50 mm, inner diameter of 40 mm and a length of 50 mm, and rotating the cylinder at 500 rpm to make the cylinder slide to each sample for 3 minutes.
- the result is shown in Table 1.
- the wear amount tends to decrease as the addition amount of WC x O y is increased. The reason for this tendency can be presumed as follows. High Young's modulus provides low distortion and deformation. Then, abnormal wear and heat due to uneven contact caused by the deformation or the like are reduced and thereby wear is restrained.
- the Young's modulus is required to be 300GPa or more.
- the examples out of the present invention including 40 volume % or less of WC x O y and the comparative examples including a simple substance of ZrO 2 have a Young's modulus of 300 MPa or less, and thereby provide inferior wear resistance.
- WC x O y is carbide having an excellent solid lubricant property, sliding wear tends to decrease as the WC x O y amount is increased. As shown in Table 1, such property is significantly exhibited by 50 volume % or more of WC x O y .
- the WC-based composite ceramics sintered body can provide materials for long-life sliding parts, edged tools or dies, excellent in mechanical and thermal properties, electrical workability and sliding properties.
- the present invention may be applied to sliding parts of a machine, edged tools for cutting polymer materials such as polyethylene or metals such as aluminum allies, press dies for bending and cutting metals or polymer materials, or the like which are required to have a high wear resistance.
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Abstract
Description
- The present invention relates to a WC-based composite ceramics sintered body used in sliding wear parts of a machine, edged tools for cutting polymer materials such as polyethylene or metals such as aluminum alloys, press dies for bending and cutting metals or polymer materials, or the like which are required to have a high wear resistance.
- Heretofore, most wear-resistant members, such as sliding wear parts of a machine, cutting blades or dies, have been formed by using ferrous metals represented by die steel. However, ZrO2-based or Si3N4-based ceramics has been recently used as a substitute for such ferrous metals having an insufficient wear resistance.
- Particularly in press working required to provide an accurate size of a finished product, since a press die tends to incur seizing with a workpiece and earlier wear-out, it is necessary to form the press die with a material having a long life and excellent wear resistance.
- As a ceramics die material having a higher hardness and superior seizing resistance in comparison with metals, Japanese Patent Publication No.
Hei 01-024747 Sho 58-120571 Hei. 03-051667 Hei 09-221352 - Required properties of the die material in case of applying ceramics to sliding wear parts, cutting blades or dies include four parameters of Young's modulus, hardness, heat conductivity and electrical workability.
- As to Young's modulus, conventional ferrous metals represented by die steel or conventional ceramics-based materials including zirconia as a primary component for providing high strength and toughness have a low Young's modulus of 2.5 GPa or less. Thus, each conventional material is insufficient in stiffness during its high-speed sliding motion with respect to an opposite member. This causes an elastic deformation of the material and excessive friction between the material and the opposite member, resulting in an abnormal wear of the material. Specifically, the ferrous materials cause an abnormal wear, while in ZrO2-based materials, the resulting frictional heat promotes crystal transformation and thereby an undesirable wear arises from fall-off of grains. This wear has an influence on usable period or life of parts. In particular, such wear would be a fatal factor in a field having a requirement of accurate motion.
- As to hardness, the advantage of ceramics compared to conventional metal-based materials is to provide an improved wear resistance based on high hardness. However, a ceramics-based die material including zirconia as a primary component is insufficient in hardness and thereby low wear resistance or short life is undesirable exhibited.
- WC includes free carbon. Thus, during a sintering process in an inert atmosphere, the free carbon remains in a sintered body, and undesirable fracture can originate in the remaining free carbon, resulting in lowered strength of the sintered body. In a ZrO2-WC composite body, ZrO2 and WC have different thermal expansion coefficients and are oxide and carbide, respectively, which are not solid-soluble each other. Thus, at a stage in which the composite body has been cooled from a high temperature in a sintered state down to a room temperature, cracks can arise from a difference in thermal expansion, and the composite body tends to fracture due to lowered mechanical properties, particularly in bending strength.
- As to heat conductivity, when heat conductivity is low, heat generated by friction during high-speed motion can be accumulated in the material, and this accumulated heat causes phase transition in zirconia as the primary component, resulting in fracture due to the transformation.
- As to electrical workability, in parallel with advancing electrical machining technologies, such as a wire-cut electric discharge machining, as well as mechanical machining technologies, many parts are recently produced by using such technologies, and it is often the case that an electrically machined surface of such parts is used as it is. However, even in the zirconia-based ceramics material enhancing hardness and conductivity, its electrically machined surface has a degraded surface roughness due to insufficient fineness and uniformity of the internal structure of the die material. As a result, the electrically machined surface could not be used as it is.
- T. Shiono et al., Journal of the Japan Society of Powder and Powder Metallurgy, Vol. 43, No. 7, July 1996, pages 885-889 discloses the preparation and mechanical properties of ZrO2-WC composites by slip-casting technique.
- K. Haberko et al., European Journal of Solid State and Inorganic Chemistry, Vol. 32, No. 7/8, 1995, pages 593-601 disclose preparation and properties of particulate composites with Y-TZP matrix and WC inclusions.
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US 5,994,250 discloses a sintered ceramic body which can be worked by electrical discharge machining which can be worked into sintered ceramic tools. - T. Venkateswaran et al., Wear 260 (2006) 1-9 discloses the processing and properties of
WC 6 weight percent ZrO2 composites. - B. Basu et al., Journal of the European Ceramic Society, Vol. 25, No. 9, pages 1603-1610 discloses pressureless sintering and tribological properties of WC-ZrO2 composites.
- It is an object of the present invention to provide a ceramic sintered body capable of sufficiently fulfilling various properties, such as Young's modulus, hardness, heat conductivity and electrical workability, which are required as materials for sliding parts, edged tools and dies.
- The present invention provides a WC-based composite ceramics sintered body according to
claim 1. Preferred embodiments are disclosed in the subclaims. According to the invention is also a method according toclaim 5. - The WC-based composite ceramics sintered body can be obtained by the following process. A pre-sintered prepared powder of raw material is held in an atmosphere containing oxygen in a temperature range of 200°C to 600°C for 0.1 hour to 3 hours to provide WC grains including solid-solved oxygen represented by a chemical formula of WCxOy (where 0.005 < y / x + y < 0.05). As a phase for filling up the grain boundary of the WC grains, partially stabilized ZrO2 is used which includes one or more of stabilizers selected from the group consisting of Y2O3, CeO2 and MgO. Then, the obtained WC is subjected to a normal sintering process or hot press sintering process in an inert gas in a temperature range of 2023 K to 2123 K to obtain the WC-based composite ceramics sintered body. Simultaneously, through the oxidizing heat treatment, free carbon in the WC grains is removed to provide an improved grain fall-off resistance, and an enhanced hardness, toughness and strength of the composite material. Further, the electrical machining operation can provide an improved electrical workability and heat conductivity with lower electric resistance.
- Modes of embodiments according to the present invention will now be described in conjunction with examples.
- A compound of raw material shown in Table 1 was prepared by providing a WC powder having an average grain size of 0.5 µm, and a predetermined amount of ZrO2 having an average grain size of 0.5 µm and partially stabilized by 3 mol % of Y2O3, as primary components, adding the predetermined amount of ZrO2 to the WC powder, and mixing the WC powder and the predetermined amount of ZrO2 for 20 hours within a nylon pot containing ZrO2 balls each comprising a sintered body having a purity of 99.5 % in a methanol solvent. The resulting slurry was taken out, and a granular powder was then prepared by adding an alcoholic binder to the slurry, and drying the slurry with the binder by a closed cycle type spray dryer in a nitrogen atmosphere.
- Samples for a bending test of 4 x 5 x 45 and samples for measuring heat conductivity of φ 20 x 3 t mm were made from the prepared granular powder through die press working, and were degreased by holding in a vacuum atmosphere at 500°C for 1 hour. After degreasing, the resulting press bodies were subjected to a heat treatment in an ambient atmosphere at 400°C for 1 hour to introduce oxygen into the WC grains. Then, the bodies were subjected to a normal sintering process in an argon gas in a temperature range of 2030 K to 2123 K. A part of the obtained samples were subjected to an HIP treatment using a nitrogen gas in a temperature range of 1923 K to 2023 K. Otherwise, the oxidizing heat treatment may be carried out to the powder of raw material or the prepared powder after granulating and drying to obtain the same effect.
- The degreased press bodies of 50 x 50 x 5 mm were put in a carbon dice and subjected to the hot press sintering process. Each sample made through two kinds of sintering processes was machined, and each heat conductivity of their mechanical properties was measured.
- The obtained samples were appropriately cut to research their solid-state properties and measure their thermal properties such as heat conductivity.
- As to the oxygen amount in WC, the ratio of C and O was determined by measuring each diffractive intensity of WC and WO3 at a low angle side in X-ray diffractions of the obtained sintered bodies.
- The above measurement results are shown in Table 1. The following effects can be proved from each of the results.
- WC grains have excellent properties of high hardness, Young's modulus, conductivity and melting point. On the other hand, due to its poor sintering property, a single substance of WC is hardly to be adequately sintered. Thus, as in hard metals, a binder phase is formed by adding a metal such as Co or Ni to finalize a sintered body structure. However, the properties of metals serving as the binder phase are significantly exhibited in evaluations of wear resistance, high temperature property which are influenced by hardness or the like. According to the present invention, using ZrO2, which has high strength and toughness among ceramics, as a substitute for the binder phase based on metals, such as Co or Ni, allows the WC grains to be sintered in approximate theoretical density.
- The content of WC depends on the sintering property varied by the addition amount of ZrO2, and it has been identified that a dense sintered body exhibiting high strength could be obtained by adding ZrO2 of 20 volume %.
- While the ZrO2 component is preferably provided as a stabilized ZrO2 obtained by adding Y2O3 of 2 to 4 mol %, a stabilized ZrO2 obtained by adding MgO or CeO2 may achieve the similar effects. However, a sufficient sintering property cannot be assured by 20 volume % or less of ZrO2. In this case, a sintered body having many pores will be provided with degraded strength and hardness. On the other hand, in 60 volume % or more of ZrO2, it has been identified that the properties of ZrO2 was significantly exhibited, and caused deteriorated hardness and wear resistance, and the grain fall-off, particular to ZrO2, due to transformation by the frictional heat, resulting in inferior sliding wear resistance.
- WC includes free carbon. Thus, during a sintering process in an atmosphere containing an inert gas such as an argon gas, the free carbon is apt to remain in the form of a lump of carbon in a sintered body, and some fracture can originate in the remaining free carbon, resulting in lowered strength of the sintered body. According to the present invention, the free carbon is removed by subjecting WC in the stage of green compact to an oxidizing heat treatment to sublimate the free carbon as a hydrocarbon compound, which enables a sintered body to assure high strength. In Table 1, the inventive examples No. 1 to 9 show a minimum strength decreasing rate of 15 % or less. While the examples No. 16 to 19 having the same composition as that of the inventive examples but the heat treatment conditions out of the inventive range show few difference in most properties, their minimum strength is lower and a decreasing rate of 25 % or more is caused by a remaining free carbon.
- WC is gradually oxidized in the temperature range of less than 600°C and the oxidization exponentially accelerates in the temperature range of 600°C or more. In parallel with the progression of the oxidization, the solid solution amount of oxygen is increased. When the value of y / x + y in WCxOy is increased to 0.05 or more, an oxide film is formed on the surface of the WC. This causes lowered strength. Further, since the oxide film has an insulative property, the electrical conductivity is deteriorated. Thus, it is preferable that the solid-solution amount of oxygen to WC is defined by WCxOy (where 0.005 < y / x + y < 0.05). As is apparent in the comparison between the inventive examples No. 1 to 9 and the examples No. 16 to 19 having the same composition as that of the inventive examples but the solid-solution amount of oxygen out of the inventive range in Table 1, there are differences in decreasing rate of strength, heat conductivity and electric resistance between them, and the examples No. 16 to 19 are inferior in wire cut surface roughness and sliding wear amount in dynamic properties.
- The reasons for excellent properties of a composite material of WC and ZrO2 are as follows.
- There is a large difference in thermal expansion coefficient between WC and ZrO2, specifically thermal expansion coefficients of WC and ZrO2 are 4 x 10-6 and 10 x 10-6, respectively. Thus, when the sintered body is cooled from a sintering temperature down to a room temperature, a certain compression stress is acted to WC and a certain tensile stress is acted to ZrO2. This provides an effect of enhancing strength and toughness of the sintered body. By virtue of combination of matrix and dispersed grains, the difference in thermal expansion is maximized in the combination of the present invention. However, this also leads to cracks. Thus, it is advantageous to effectively restrain such cracks by arranging the solid-solution amount of oxygen to WC in WCxOy (where 0.005 < y / x + y < 0.05) to provide stress relaxation in grain boundary.
- Differently from hard metals including Co or Ni, ceramics is densified in solid-phase sintering, not in liquid-phase sintering, during a sintering process. For example, in solid-phase sintering between Al2O3 and WC, Al2O3 acts as a rate-limiting factor of sintering. Thus, any plastic flow is caused during crystal structure is densified, and thereby pores are apt to remain. However, in the combination of WCx Oy and ZrO2 according to the present invention, a superplasticity phenomenon appears in the sintering temperature of ZrO2, and a structure in which ZrO2 gets into a space between crystals is formed to provide enhanced density. In this case, the density is more enhanced by using WCx Oy which includes a few amount of solid-solved oxygen, as compared with using only WC. Thus, an adequate sintering can be achieved by less amount of ZrO2 than that in combination of only WC and ZrO2.
- As described above, in the combination of WCx Oy and ZrO2 grains of the present invention, WCx Oy and ZrO2 grains are dispersed in an individually independent form without any mutual reaction. Further, since WCx Oy is matrix and ZrO2 functions to restrain grain growth as with the function of a grain boundary binding phase. This allows WC and ZrO2 to be uniformly dispersed respectively. In addition, by virtue of generation of residual stress, as compared to conventional ceramics, enhanced values of strength, toughness and hardness are exhibited. More excellent thermal and electrical properties than ever are also provided. As shown in Table 1, when Al2O3 having lower thermal expansion coefficient than that of ZrO2 is mixed to WCx Oy, each improvement in the properties is small. This can verify that the composite material of WCx Oy and ZrO2 is more effective.
- In particular, the composite material has a Young's modulus of 300 MPa or more, which is 1.5 times or more of that of ZrO2-based ceramics or metals, and can assure the same stiffness as that of Si3N4. For example, if this composite material is applied to high-speed motion mechanisms such as bearing and sleeve, or high-speed press machines, lowered distortion and deformation, restrained frictional heat, and reduced sliding wear can be achieved.
- As to thermal properties, ceramics including a large amount of ZrO2 has low heat conductivity. In contrast, since the composite material according to the present invention includes WC having high heat conductivity as a primary component, a sufficient heat conductivity being ten times of that of a simple substance of ZrO2 is obtained to provide an improved thermal shock resistance against rapid heating and cooling.
- WCx Oy itself has a high conductivity. Thus, larger WCx Oy amount, less electric resistance value. As to heat conductivity, an electrical machining such as a wire-cut electric discharge machining can be applied to a composite material including 30 volume % or more of WCx Oy. In this case, it has been proved that surface roughness of the electrically machined surface was influenced by the conductivity of the composite material and the dispersed degree of conductive grains. As shown in Table 1, it has been identified that 50 volume % or more of WCx Oy could provide an improved surface roughness of the electrically machined surface.
- In the material of the present invention, mechanical, thermal and electrical properties are influenced a great deal by the dispersion state of each components of the composite material. Agglomerates of WCx Oy or ZrO2 are left as a defect originating fracture. As to electrical properties, agglomerates of ZrO2 cannot be electrically machined and is thereby left as a crude portion. As to sliding wear, the agglomerates of WCx Oy or ZrO2 cause abnormal wear. Thus, each agglomerate of WCx Oy and ZrO2 is required to limit to 10 µm or less when converting into diameter of the same area, and to 3 or less per mm2 in its number.
- In the wear test, each wear value was measured by inserting each sample of the inventive materials and comparative materials each having an outer diameter of 40 mm, inner diameter of 30 mm and a length of 50 mm, into an inside of a hard metal cylinder having an outer diameter of 50 mm, inner diameter of 40 mm and a length of 50 mm, and rotating the cylinder at 500 rpm to make the cylinder slide to each sample for 3 minutes. The result is shown in Table 1. The wear amount tends to decrease as the addition amount of WCx Oy is increased. The reason for this tendency can be presumed as follows. High Young's modulus provides low distortion and deformation. Then, abnormal wear and heat due to uneven contact caused by the deformation or the like are reduced and thereby wear is restrained. The Young's modulus is required to be 300GPa or more. The examples out of the present invention including 40 volume % or less of WCx Oy and the comparative examples including a simple substance of ZrO2 have a Young's modulus of 300 MPa or less, and thereby provide inferior wear resistance. Further, since WCxOy is carbide having an excellent solid lubricant property, sliding wear tends to decrease as the WCx Oy amount is increased. As shown in Table 1, such property is significantly exhibited by 50 volume % or more of WCx Oy. The WC-based composite ceramics sintered body can provide materials for long-life sliding parts, edged tools or dies, excellent in mechanical and thermal properties, electrical workability and sliding properties.
- The present invention may be applied to sliding parts of a machine, edged tools for cutting polymer materials such as polyethylene or metals such as aluminum allies, press dies for bending and cutting metals or polymer materials, or the like which are required to have a high wear resistance.
Claims (5)
- A WC-based composite ceramics sintered body consisting of 40 volume % to 90 volume % of WC which includes solid-solved oxygen and from which free carbon is removed to hava a chemical formula represented by WCxOy (where 0.005 < y / x + y < 0.05), with the remainder being partially stabilized ZrO2 and inevitable impurities, said partially stabilized ZrO2 includes one or more of stabilizers selected from the group consisting of Y2O3, CeO2 and MgO, wherein WCxOy and ZrO2 grains are dispersed in an individually independent form.
- A WC-based composite ceramics sintered body as defined in claim 1, wherein agglomerates of either one of WCxOy (where 0.005 < y / x + y < 0.05) and ZrO2 in said sintered body respectively have a diameter of 3 µm to 10 µm when said diameter is converted into a diameter of a sphere having the same volume as that of each agglomerate, and the number of said agglomerates are 3 or less per mm3.
- A WC-based composite ceramics sintered body as defined in claim 1, which has a Young's modulus of 300 GPa or more.
- A WC-based composite ceramics sintered body as defined in claim 1, which has a heat conductivity of 20 W / m · K or more.
- A manufacturing method of a WC-based composite ceramics sintered body, comprising:holding a mixed powder consisting of 40 volume % to 90 volume % of WC, with the remainder being partially stabilized ZrO2 including one or more of stabilizers selected from the group consisting of Y2O3, CeO2 and MgO, in an atmosphere containing oxygen in a temperature range of 200°C to 600°C for 0.1 hour to 3 hours to provide WC which includes solid-solved oxygen and from which free carbon is removed to have a chemical formula represented by WCxOy (where 0.005 < y / x + y < 0.05); andsintering said resulting mixed powder to obtain the WC-based composite ceramics sintered body having said WCxOy and said ZrO2 grains which are dispersed therein in an individually independent form.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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JP30604999 | 1999-10-27 | ||
JP30604999A JP4598212B2 (en) | 1999-10-27 | 1999-10-27 | Method for producing WC-based composite ceramic sintered body |
PCT/JP2000/007477 WO2001030722A1 (en) | 1999-10-27 | 2000-10-26 | Wc-base composite ceramic sintered compact |
Publications (3)
Publication Number | Publication Date |
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EP1146025A1 EP1146025A1 (en) | 2001-10-17 |
EP1146025A4 EP1146025A4 (en) | 2006-06-07 |
EP1146025B1 true EP1146025B1 (en) | 2012-06-20 |
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EP00970077A Expired - Lifetime EP1146025B1 (en) | 1999-10-27 | 2000-10-26 | Wc-base composite ceramic sintered compact |
Country Status (4)
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US (1) | US6551954B1 (en) |
EP (1) | EP1146025B1 (en) |
JP (1) | JP4598212B2 (en) |
WO (1) | WO2001030722A1 (en) |
Families Citing this family (9)
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JP4598212B2 (en) * | 1999-10-27 | 2010-12-15 | 日本タングステン株式会社 | Method for producing WC-based composite ceramic sintered body |
JP4700217B2 (en) * | 2001-04-26 | 2011-06-15 | 日本タングステン株式会社 | WC-ZrO2-based composite ceramic sintered body |
CN100425371C (en) * | 2005-01-19 | 2008-10-15 | 鸿富锦精密工业(深圳)有限公司 | Wear resistant appliance and preparation method thereof |
CN101181754B (en) * | 2007-11-30 | 2010-06-30 | 东华大学 | Method for preparing WC/MgO nano composite powder |
CN106631024A (en) * | 2016-12-27 | 2017-05-10 | 郑州源冉生物技术有限公司 | High-performance tungsten carbide ceramic material |
JP7329323B2 (en) * | 2018-12-07 | 2023-08-18 | 日本特殊陶業株式会社 | Ceramic sintered bodies, inserts, cutting tools, and tools for friction stir welding |
CN110342907B (en) * | 2019-07-22 | 2023-02-14 | 中国科学院上海光学精密机械研究所 | Preparation method of Y2O3-MgO nano complex phase infrared ceramic |
CN111848168B (en) * | 2020-07-29 | 2022-03-18 | 台州学院 | A method for preparing WC-Y2O3 binderless phase cemented carbide by in-situ reactive hot pressing sintering |
CN115108834B (en) * | 2022-07-21 | 2023-09-26 | 燕山大学 | Tungsten carbide sintered body and preparation method thereof |
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US4828584A (en) * | 1986-01-09 | 1989-05-09 | Ceramatec, Inc. | Dense, fine-grained tungsten carbide ceramics and a method for making the same |
JPS62288166A (en) * | 1986-06-03 | 1987-12-15 | 松下電器産業株式会社 | Manufacture of tungsten carbide-oxide composite sintered body |
JPH0832587B2 (en) * | 1989-04-10 | 1996-03-29 | 日本タングステン株式会社 | Ceramics sintered body and its manufacturing method |
JP3145470B2 (en) * | 1992-03-31 | 2001-03-12 | 京セラ株式会社 | Tungsten carbide-alumina sintered body and method for producing the same |
JP3541108B2 (en) | 1995-11-07 | 2004-07-07 | 日本特殊陶業株式会社 | Ceramic sintered body and ceramic mold |
JP4598212B2 (en) * | 1999-10-27 | 2010-12-15 | 日本タングステン株式会社 | Method for producing WC-based composite ceramic sintered body |
-
1999
- 1999-10-27 JP JP30604999A patent/JP4598212B2/en not_active Expired - Fee Related
-
2000
- 2000-10-26 EP EP00970077A patent/EP1146025B1/en not_active Expired - Lifetime
- 2000-10-26 WO PCT/JP2000/007477 patent/WO2001030722A1/en active Application Filing
- 2000-10-26 US US09/869,241 patent/US6551954B1/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
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WO2001030722A1 (en) | 2001-05-03 |
EP1146025A4 (en) | 2006-06-07 |
EP1146025A1 (en) | 2001-10-17 |
US6551954B1 (en) | 2003-04-22 |
JP2001122664A (en) | 2001-05-08 |
JP4598212B2 (en) | 2010-12-15 |
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